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通过一种新型的“以疾病为重点的诊断审查”质量改进流程,提高病理学家在解决前列腺活检中“可疑癌症的非典型腺体”诊断方面的诊断一致性。

Improvement of diagnostic agreement among pathologists in resolving an "atypical glands suspicious for cancer" diagnosis in prostate biopsies using a novel "Disease-Focused Diagnostic Review" quality improvement process.

作者信息

Shah Rajal B, Leandro Gioacchino, Romerocaces Gloria, Bentley James, Yoon Jiyoon, Mendrinos Savvas, Tadros Yousef, Tian Wei, Lash Richard

机构信息

Division of Pathology, Miraca Life Sciences, Irving, TX 75039.

IRCC De Bellis, Gastroenterology, Castellana Grotte, Italy.

出版信息

Hum Pathol. 2016 Oct;56:155-62. doi: 10.1016/j.humpath.2016.06.009. Epub 2016 Jun 23.

Abstract

One of the major goals of an anatomic pathology laboratory quality program is to minimize unwarranted diagnostic variability and equivocal reporting. This study evaluated the utility of Miraca Life Sciences' "Disease-Focused Diagnostic Review" (DFDR) quality program in improving interobserver diagnostic reproducibility associated with classification of "atypical glands suspicious for adenocarcinoma" (ATYP) in prostate biopsies. Seventy-one selected prostate biopsies with a focus of ATYP were reviewed by 8 pathologists. Participants were blinded to the original diagnosis and were first asked to classify the ATYP as benign, atypical, or limited adenocarcinoma. DFDR comprised a "theoretical consensus" (in which pathologists first reached consensus on the morphological features they considered relevant for the diagnosis of limited prostatic adenocarcinoma), a didactic review including relevant literature, and "practical consensus" (pathologists performed joint microscopic sessions, reconciling each other's observations and positions evaluating a separate unique slide set). Participants were finally asked to reclassify the original 71 ATYP cases based on knowledge gleaned from DFDR. Pre- and post-DFDR interobserver reproducibility of overall diagnostic agreement was assessed. Interobserver reproducibility measured by Fleiss κ values of pre- and post-DFDR was 0.36 and 0.59, respectively (P=.006). Post-DFDR, there were significant improvement for "100% concordance" (P=.011) and reduction for "no consensus" (P=.0004) categories. Despite a lower pre-DFDR reproducibility for non-uropathology fellowship-trained (n=3, κ=0.38) versus uropathology fellowship-trained (n=5, κ=0.43) pathologists, both groups achieved similarly high post-DFDR κ levels (κ=0.58 and 0.56, respectively). DFDR represents an effective tool to formally achieve diagnostic consensus and reduce variability associated with critical diagnoses in an anatomic pathology practice.

摘要

解剖病理学实验室质量计划的主要目标之一是尽量减少不必要的诊断变异性和模棱两可的报告。本研究评估了Miraca生命科学公司的“疾病聚焦诊断审查”(DFDR)质量计划在提高与前列腺活检中“可疑腺癌的非典型腺体”(ATYP)分类相关的观察者间诊断可重复性方面的效用。8名病理学家对71例选定的以ATYP为重点的前列腺活检进行了复查。参与者对原诊断不知情,首先被要求将ATYP分类为良性、非典型或局限性腺癌。DFDR包括“理论共识”(病理学家首先就他们认为与局限性前列腺腺癌诊断相关的形态学特征达成共识)、包括相关文献的教学回顾以及“实际共识”(病理学家进行联合显微镜检查,协调彼此对单独一组独特玻片的观察和判断)。最后要求参与者根据从DFDR中学到的知识对最初的71例ATYP病例重新分类。评估了DFDR前后观察者间总体诊断一致性的可重复性。DFDR前后通过Fleiss κ值测量的观察者间可重复性分别为0.36和0.59(P = 0.006)。DFDR后,“100%一致性”类别有显著改善(P = 0.011),“无共识”类别有所减少(P = 0.0004)。尽管未接受泌尿病理学专科培训的病理学家(n = 3,κ = 0.38)在DFDR前的可重复性低于接受泌尿病理学专科培训的病理学家(n = 5,κ = 0.43),但两组在DFDR后的κ水平都同样高(分别为κ = 0.58和0.56)。DFDR是在解剖病理学实践中正式达成诊断共识并减少与关键诊断相关的变异性的有效工具。

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